Leveraging population-scale long-read sequencing to uncover structural variants driving disease associations: insights from the All of Us initiative
April 16, 2026 - April 17, 2026
Thursday, April 16, 8:00 AM PDT | 11:00 AM EDT | 4:00 PM BST
Friday, April 17, 11:00 AM SGT | 1:00 PM AEST
Join Dr. Michael Schatz (Johns Hopkins University) as he unpacks how PacBio HiFi whole genome sequencing (WGS) is being applied across diverse populations. Drawing on insights from the All of Us initiative, he highlights how long-read WGS uncovers previously hidden variants and what that means for discovery at scale.